# BENZPHETAMINE HYDROCHLORIDE

NDC: 43063-541
Generic name: benzphetamine hydrochloride
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100721

FDA application: ANDA090968

## Active ingredients

- BENZPHETAMINE HYDROCHLORIDE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-541"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-541
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2b7014af-0cc9-4199-90f2-ec07ac02f8cf